rs76449634

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs76449634(C;T)

Make rs76449634(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43102542

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs76449634
dbSNP (classic)	rs76449634
ClinGen	rs76449634
ebi	rs76449634
HLI	rs76449634
Exac	rs76449634
Gnomad	rs76449634
Varsome	rs76449634
LitVar	rs76449634
Map	rs76449634
PheGenI	rs76449634
Biobank	rs76449634
1000 genomes	rs76449634
hgdp	rs76449634
ensembl	rs76449634
geneview	rs76449634
scholar	rs76449634
google	rs76449634
pharmgkb	rs76449634
gwascentral	rs76449634
openSNP	rs76449634
23andMe	rs76449634
SNPshot	rs76449634
SNPdbe	rs76449634
MSV3d	rs76449634
GWAS Ctlg	rs76449634

Max Magnitude

0

OMIM	164761
Desc
Variant	0021
Related	also

ClinVar
Risk	rs76449634(T;T)
Alt	rs76449634(T;T)
Reference	Rs76449634(C;C)
Significance	Other
Disease	Hirschsprung disease 1
Variation	info
Gene	RET
CLNDBN	Hirschsprung disease 1
Reversed	0
HGVS	NC_000010.10:g.43597990C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014950.2,